Canonical Allele Identifier: CA891842976

Gene: NR3C2

Linked Data

• ClinVar Variation Id: 8560
• ClinVar RCV Id: RCV000009091
• dbSNP Id: rs1560735659
• MyVariant Identifiers: chr4:g.149356882dup (hg19) ; chr4:g.148435730dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148435730dup , CM000666.2:g.148435730dup	GRCh38
NC_000004.11:g.149356882dup , CM000666.1:g.149356882dup	GRCh37
NC_000004.10:g.149576332dup	NCBI36
NG_013350.1:g.11791dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.1131dup MANE Select	ENSP00000350815.3:p.Glu378Ter
ENST00000342437.8:c.1131dup	ENSP00000343907.4:p.Glu378Ter
ENST00000344721.8:c.1131dup	ENSP00000341390.4:p.Glu378Ter
ENST00000358102.7:c.1131dup	ENSP00000350815.3:p.Glu378Ter
ENST00000511528.1:c.1131dup	ENSP00000421481.1:p.Glu378Ter
ENST00000512865.5:c.1131dup	ENSP00000423510.1:p.Glu378Ter
ENST00000625323.2:c.1131dup	ENSP00000486719.1:p.Glu378Ter
NM_000901.4:c.1131dup	NP_000892.2:p.Glu378Ter
NM_001166104.1:c.1131dup	NP_001159576.1:p.Glu378Ter
XM_011531975.1:c.1131dup	XP_011530277.1:p.Glu378Ter
XM_011531976.1:c.1131dup	XP_011530278.1:p.Glu378Ter
XM_011531977.1:c.1131dup	XP_011530279.1:p.Glu378Ter
XM_011531978.1:c.1131dup	XP_011530280.1:p.Glu378Ter
NM_001354819.1:c.1131dup	NP_001341748.1:p.Glu378Ter
NR_148974.1:n.1494dup
XM_011531978.2:c.1131dup	XP_011530280.1:p.Glu378Ter
NM_000901.5:c.1131dup MANE Select	NP_000892.2:p.Glu378Ter
NM_001166104.2:c.1131dup	NP_001159576.1:p.Glu378Ter
NR_148974.2:n.1388dup